ENST00000350026.11:c.4740C>G
|
ENSP00000055163.8:p.Ser1580Arg
|
|
ENST00000414678.8:c.4809C>G
|
ENSP00000412835.3:p.Ser1603Arg
|
|
ENST00000637015.2:c.5028C>G
|
ENSP00000489729.2:p.Ser1676Arg
|
|
ENST00000346085.10:c.4779C>G
|
ENSP00000344546.5:p.Ser1593Arg
|
|
ENST00000350026.10:c.4491C>G
|
ENSP00000055163.7:p.Ser1497Arg
|
|
ENST00000414678.7:c.3057C>G
|
ENSP00000412835.2:p.Ser1019Arg
|
|
ENST00000635849.1:c.2220C>G
|
ENSP00000490948.1:p.Ser740Arg
|
|
ENST00000635957.1:c.1851C>G
|
ENSP00000490385.1:p.Ser617Arg
|
|
ENST00000636227.1:n.3362C>G
|
|
|
ENST00000636254.1:n.819C>G
|
|
|
ENST00000636930.2:c.4899C>G
MANE Select
|
ENSP00000490491.2:p.Ser1633Arg
|
|
ENST00000636940.1:n.2896C>G
|
|
|
ENST00000637015.1:c.2267C>G
|
|
|
ENST00000637568.1:c.2181C>G
|
|
|
ENST00000637741.1:n.1565C>G
|
|
|
ENST00000637810.1:c.2241C>G
|
ENSP00000489636.1:p.Ser747Arg
|
|
ENST00000637904.1:c.2400C>G
|
ENSP00000490550.1:p.Ser800Arg
|
|
ENST00000647938.1:c.4530C>G
|
ENSP00000498155.1:p.Ser1510Arg
|
|
ENST00000346085.9:c.4530C>G
|
ENSP00000344546.4:p.Ser1510Arg
|
|
ENST00000350026.9:c.4491C>G
|
ENSP00000055163.7:p.Ser1497Arg
|
|
ENST00000414678.6:c.3057C>G
|
ENSP00000412835.2:p.Ser1019Arg
|
|
NM_017519.2:c.4491C>G
|
NP_059989.2:p.Ser1497Arg
|
|
NM_020732.3:c.4530C>G
|
NP_065783.3:p.Ser1510Arg
|
|
XM_005267069.3:c.4650C>G
|
XP_005267126.2:p.Ser1550Arg
|
|
XM_011535984.1:c.3729C>G
|
XP_011534286.1:p.Ser1243Arg
|
|
XM_011535985.1:c.3549C>G
|
XP_011534287.1:p.Ser1183Arg
|
|
XM_011535986.1:c.3309C>G
|
XP_011534288.1:p.Ser1103Arg
|
|
XM_011535987.1:c.2928C>G
|
XP_011534289.1:p.Ser976Arg
|
|
XM_011535988.1:c.1791C>G
|
XP_011534290.1:p.Ser597Arg
|
|
NM_001346813.1:c.4650C>G
|
NP_001333742.1:p.Ser1550Arg
|
|
NM_001363725.1:c.2400C>G
|
NP_001350654.1:p.Ser800Arg
|
|
XM_011535984.2:c.4860C>G
|
XP_011534286.2:p.Ser1620Arg
|
|
XM_011535988.3:c.1791C>G
|
XP_011534290.1:p.Ser597Arg
|
|
XM_017011103.2:c.4761C>G
|
XP_016866592.1:p.Ser1587Arg
|
|
XM_017011104.1:c.4731C>G
|
XP_016866593.1:p.Ser1577Arg
|
|
XM_017011105.2:c.4701C>G
|
XP_016866594.1:p.Ser1567Arg
|
|
XM_017011106.2:c.4572C>G
|
XP_016866595.1:p.Ser1524Arg
|
|
XM_017011107.2:c.4551C>G
|
XP_016866596.1:p.Ser1517Arg
|
|
XR_002956289.1:n.4846C>G
|
|
|
NM_001363725.2:c.2400C>G
|
NP_001350654.1:p.Ser800Arg
|
|
NM_001371656.1:c.4779C>G
|
NP_001358585.1:p.Ser1593Arg
|
|
NM_001374820.1:c.4779C>G
|
NP_001361749.1:p.Ser1593Arg
|
|
NM_001374828.1:c.4899C>G
MANE Select
|
NP_001361757.1:p.Ser1633Arg
|
|
NM_017519.3:c.4740C>G
|
NP_059989.3:p.Ser1580Arg
|
|